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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712428Generated: October 29, 2026

Formaldehyde → HCID 71572548, compound

https://huagongshe.com/reaction/712428

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantMethanolHCID 887—
ReactantDichloromethaneHCID 6344—
ReactantHCID 86729479HCID 86729479—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductHCID 71572548HCID 7157254876.2%

Reaction Steps

To a solution of tert-butyl 6-(3-((4-((3-chloro-4-fluorophenyl)amino)-7-methoxyquinazolin-6-yl)oxy) propyl)octahydro-1H-pyrrolo[2,3-c]pyridine-1-carboxylate (0.20 g) in the mixture solvent of CH2Cl2 and MeOH was added 37% HCHO (0.10 mL), AcOH (0.15 mL) and NaB(O2CCH3)3H (0.26 g) in turn at room temperature. The mixture was stirred for 1.5 h, diluted with water and extracted with CH2Cl2. The organic layer was dried over anhydrous Na2SO4 for 1 h and filtered. The filtrate was concentrated and redissolved in EA, to this, a solution of HCl in EtOAc (10 mL) was added under stirring. The mixture was filtered to give the title compound as a solid (0.13 g, 68.00%), HPLC: 98.22%. The compound was characterized by the following spectroscopic data: MS (ESI, pos. ion) m/z: 500.2 (M+1); 1H NMR (400 MHz, CDCl3) δ: 1.45 (m, 2H), 1.68 (m, 3H), 1.80 (m, 2H), 2.10 (m, 1H), 2.22 (m, 5H), 2.25 (s, 3H), 2.42 (m, 3H), 4.03 (s, 3H), 4.10 (m, 2H), 6.76 (s, 1H), 7.16 (d, J=8.2 Hz, 1H), 7.24 (s, 1H), 7.28 (d, J=8.0 Hz, 1H), 7.41 (s, 1H), 8.54 (s, 1H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181277B2
Source datasetuspto-grants-2015_11
ORD IDord-c8291b66ec644b9fb447dcd3bfe8c462
Source noteuspto-grants-2015_11