Hydrogen chloride-ethyl acetate → HCID 14689279, compound

HRID 1399858Notes

Reaction equation

HRID 1399858 reaction equation
[CH2:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH2:3][N:2]1[CH2:11][CH:12]([OH:29])[CH2:13][O:14][C:15]1[CH:16]=[C:17]([NH:21]C(=O)OC(C)(C)C)[CH:18]=[CH:19][CH:20]=1.Cl.C(OCC)(=O)C>C(OCC)(=O)C>[NH2:21][C:17]1[CH:16]=[C:15]([CH:20]=[CH:19][CH:18]=1)[O:14][CH2:13][CH:12]([OH:29])[CH2:11][N:2]1[CH2:3][CH2:4][C:5]2[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=2)[CH2:1]1

Participants

4

Procedure

To a solution of tert-butyl (3-(3-(3,4-dihydroisoquinolin-2(1H)-yl)-2-hydroxypropoxy)phenyl)carbamate (1.2 g, 3.01 mmol) in ethyl acetate (30 mL) was added HCl/ethyl acetate (20 mL). The reaction mixture was stirred at room temperature for 2 h. and the concentrated with the residue used in the next step without further purification.

Workup

  1. concentrationthe concentrated with the residue
  2. customused in the next step without further purification

Sources & evidence

ORD record
ord-923c2e884a084718817db13fef882991
Source dataset
uspto-grants-2014_12
Patent number
US08906900B2

Reaction notes

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