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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350143Generated: November 2, 2026

Formaldehyde → HCID 69321373, compound

https://huagongshe.com/reaction/1350143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 69319657HCID 69319657—
SolventAcetic AcidHCID 176—
ProductHCID 69321373HCID 6932137393%

Reaction Steps

This compound was prepared by General Method 5 (EXAMPLE 1) from (3R)-3-ethyl-3,4-dihydro-8-isopropoxy-10-(trifluoromethyl)-2H-[1,4]oxazino[2,3-f]quinoline (0.015 g, 0.044 mmol), paraformaldehyde (0.013 g, 0.44 mmol) and NaCNBH3 (0.014 g, 0.22 mmol) in 1 mL glacial acetic acid to afford 0.014 g (93%) of (3R)-3-ethyl-3,4-dihydro-8-isopropoxy-4-methyl-10-(trifluoromethyl)-2H-[1,4]oxazino[2,3-f]quinoline, of sufficient purity as to be used directly in the next reaction. Rf0.5 (9:1 hexane:EtOAc); 1H NMR (400 MHz, CDCl3) δ 7.44 (d, 1H, J=9.0), 7.20 (d, 1H, J=9.0), 7.18 (s, 1H), 5.48 (septet, 1H, J=6.2), 4.29 (dd, ABX, 1H, J=10.7, 2.5), 4.02 (dd, ABX, 1H, J=10.7, 2.7), 3.21–3.16 (m, 1H), 3.03 (s, 3H), 1.74–1.56 (m, 2H), 1.39 (d, 3H, J=6.2), 1.37 (d, 3H, J=6.2), 0.99 (t, 3H, J=7.5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214690B2
Source datasetuspto-grants-2007_05
ORD IDord-1471dac3cac7436db2e5978a44109a7c
Source noteuspto-grants-2007_05