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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1294632Generated: October 30, 2026

Formaldehyde → HCID 11212985, compound

https://huagongshe.com/reaction/1294632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium HydroxideHCID 14798—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 11292979HCID 11292979—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
SolventAcetonitrile methylene chlorideHCID 21877088—
ProductHCID 11212985HCID 1121298527.8%

Reaction Steps

To a stirred solution of benzo[1,2,5]thiadiazole-4-sulfonic acid [5-amino-2-(piperidine-1-carbonyl)-phenyl]-amide (EXAMPLE 24; 30 mg, 0.072 mmol) in 2:1 acetonitrile/DCM (6 mL), was added formaldehyde (0.1 mL, 3.6 mmol), sodium cyanoborohydride (68 mg, 1.08 mmol) and acetic acid (12 μL). The reaction mixture was stirred for 3 h at room temperature. 1 M NaOH was added until the solution became basic. The mixture was taken up in DCM (5 mL), and washed with water and brine. The organic layer was removed, dried, and purified by preparative reversed-phase HPLC to afford the title compound (8 mg, 0.02 mmol, 25%). MS (ESI): m/z 446 [M+H]+, 468 [M+Na]+. HPLC (reversed-phase): RT=9.14 min (single peak). 1H NMR (400 MHz, CDCl3): (rotameric broadening) 9.61 (s, 1H), 8.22 (dd, J=7.0, 1.0 Hz, 1H), 8.18 (dd, J=8.8, 1.0 Hz, 1H), 7.63 (dd, J=8.8, 7.0 Hz, 1H), 6.95 (d, J=7.0, 2.5 Hz, 1H), 6.90 (d, J=8.7 Hz, 1H), 6.26 (dd, 8.7, 2.5 Hz, 1H), 3.16 (s, 4H), 2.95 (s, 6H), 1.56 (m, 2H), 1.42 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07241759B2
Source datasetuspto-grants-2007_07
ORD IDord-5eb97ca6159b4e05a106f32b3ed82f34
Source noteuspto-grants-2007_07